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Dynamin 1-Like Antikörper (pSer616) (Biotin)

DNM1L Reaktivität: Maus ELISA, IHC (p), IHC (fro) Wirt: Kaninchen Polyclonal Biotin
Produktnummer ABIN6943119
  • Target Alle Dynamin 1-Like (DNM1L) Antikörper anzeigen
    Dynamin 1-Like (DNM1L)
    Bindungsspezifität
    • 22
    • 11
    • 7
    • 5
    • 4
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    pSer616
    Reaktivität
    • 58
    • 52
    • 36
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Maus
    Wirt
    • 64
    • 8
    Kaninchen
    Klonalität
    • 64
    • 8
    Polyklonal
    Konjugat
    • 32
    • 5
    • 4
    • 3
    • 3
    • 3
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser Dynamin 1-Like Antikörper ist konjugiert mit Biotin
    Applikation
    • 33
    • 26
    • 18
    • 13
    • 13
    • 12
    • 9
    • 7
    • 4
    • 2
    • 2
    • 2
    ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
    Kreuzreaktivität
    Maus
    Homologie
    Human,Rat,Dog,Pig,Guinea Pig
    Aufreinigung
    Purified by Protein A.
    Immunogen
    KLH conjugated synthesised phosphopeptide derived from human DRP1 around the phosphorylation site of Ser616
    Isotyp
    IgG
    Top Product
    Discover our top product DNM1L Primärantikörper
  • Applikationshinweise
    IHC-P 1:200-400
    IHC-F 1:100-500
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Konservierungsmittel
    ProClin
    Vorsichtsmaßnahmen
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    Store at -20°C for 12 months.
    Haltbarkeit
    12 months
  • Target
    Dynamin 1-Like (DNM1L)
    Andere Bezeichnung
    DRP1 (DNM1L Produkte)
    Synonyme
    DLP1 antikoerper, DRP1 antikoerper, DVLP antikoerper, DYMPLE antikoerper, EMPF antikoerper, HDYNIV antikoerper, 6330417M19Rik antikoerper, AI450666 antikoerper, Dlp1 antikoerper, Dnmlp1 antikoerper, Drp1 antikoerper, python antikoerper, Dnml1 antikoerper, dnm1l antikoerper, MGC53850 antikoerper, zgc:66163 antikoerper, DNM1L antikoerper, 18.m06247 antikoerper, CG3210 antikoerper, DRP antikoerper, Dmel\CG3210 antikoerper, Dnm1/Drp1 antikoerper, Drp antikoerper, Drp-1 antikoerper, drp-1 antikoerper, drp1 antikoerper, frat antikoerper, l(2)22Fc antikoerper, l(2)22Fd antikoerper, l(2)ND2 antikoerper, l(2)ND3 antikoerper, dynamin 1 like antikoerper, dynamin 1-like antikoerper, dynamin 1-like L homeolog antikoerper, dynamin-1-like antikoerper, dynamin-1-like protein antikoerper, dynamin-like protein antikoerper, Dynamin related protein 1 antikoerper, DNM1L antikoerper, Dnm1l antikoerper, dnm1l.L antikoerper, dnm1l antikoerper, LOC100369408 antikoerper, LOC411472 antikoerper, dyn1 antikoerper, cgd1_580 antikoerper, EHI_052740 antikoerper, PVX_092875 antikoerper, BBOV_II002980 antikoerper, Drp1 antikoerper
    Hintergrund

    Synonyms: DRP1 (phospho S616), p-DRP1 (phospho S616), P-DRP1 (Ser616), DLP1, dnm1l, DNM1L_HUMAN, Dnm1p/Vps1p-like protein, DVLP, Dymple, Dynamin 1 like, Dynamin family member proline-rich carboxyl-terminal domain less, Dynamin like protein, Dynamin related protein 1, Dynamin-1-like protein, Dynamin-like protein 4, Dynamin-like protein, Dynamin-like protein IV, Dynamin-related protein 1, DYNIV 11, FLJ41912, HdynIV, VPS1.

    Background: This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Jun 2013]

    Gen-ID
    10059
    UniProt
    O00429
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